Persistent behavioral effects following early life exposure to retinoic acid or valproic acid in zebrafish.

Journal Article (Journal Article)

BACKGROUND: Moderate to severe dysregulation in retinoid signaling during early development is associated with a constellation of physical malformations and/or neural tube defects, including spina bifida. It is thought that more subtle dysregulation of this system, which might be achievable via dietary (i.e. hypervitaminosis A) or pharmacological (i.e. valproic acid) exposure in humans, will manifest on behavioral domains including sociability, without overt physical abnormalities. METHODS: During early life, zebrafish were exposed to low doses of two chemicals that disrupt retinoid signaling. From 0 to 5dpf, larvae were reared in aqueous solutions containing retinoic acid (0, 0.02, 0.2 or 2nM) or valproic acid (0, 0.5, 5.0 or 50μM). One cohort of zebrafish was assessed using a locomotor activity screen at 6-dpf; another was reared to adulthood and assessed using a neurobehavioral test battery (startle habituation, novel tank exploration, shoaling, and predator escape/avoidance). RESULTS: There was no significant increase in the incidence of physical malformation among exposed fish compared to controls. Both retinoic acid and valproic acid exposures during development disrupted larval activity with persisting behavioral alterations later in life, primarily manifesting as decreased social affiliation. CONCLUSIONS: Social behavior and some aspects of motor function were altered in exposed fish; the importance of examining emotional or psychological consequences of early life exposure to retinoid acting chemicals is discussed.

Full Text

Duke Authors

Cited Authors

  • Bailey, JM; Oliveri, AN; Karbhari, N; Brooks, RAJ; De La Rocha, AJ; Janardhan, S; Levin, ED

Published Date

  • January 2016

Published In

Volume / Issue

  • 52 /

Start / End Page

  • 23 - 33

PubMed ID

  • 26439099

Pubmed Central ID

  • PMC4753107

Electronic International Standard Serial Number (EISSN)

  • 1872-9711

Digital Object Identifier (DOI)

  • 10.1016/j.neuro.2015.10.001


  • eng

Conference Location

  • Netherlands